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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22348생성일: 2026년 10월 23일

Ethanol → 2,3-dihydro-7-methoxy-8-{3-[4-(3-methoxyphenyl)-1-piperazinyl]propoxy}cyclopenta[c][1]benzopyran-4(1H)-one

https://huagongshe.com/ko/reaction/22348

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물N-(3-methoxyphenyl)piperazineHCID 81430—
반응물FumarateHCID 5460307—
반응물8-(3-chloropropoxy)-2,3-dihydro-7-methoxycyclopenta[c][1]benzopyran-4(1H)-oneHCID 19927690—
용매AcetoneHCID 180—
용매IsopropanolHCID 3776—
생성물2,3-dihydro-7-methoxy-8-{3-[4-(3-methoxyphenyl)-1-piperazinyl]propoxy}cyclopenta[c][1]benzopyran-4(1H)-oneHCID 1992767958%

반응 단계

Method B (60 h at 50° C.); starting materials: 8-(3-chloropropoxy)-2,3-dihydro-7-methoxy-cyclopenta[c][1]benzopyran-4(1H)-one (example 83) and 1-(3-methoxyphenyl)piperazine; yield 58%; fusion point 130°-132° C. (from ethanol and isopropanol). Fumarate: method E; yield 80%; fusion point 174°-175° C. (from acetone).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05428038
출처 데이터셋uspto-grants-1995_06
ORD IDord-eb759a0b34b746ed8ab96923d5d5c27c
출처 메모uspto-grants-1995_06